FDA 510(k) Application Details - K172333

Device Classification Name	System, Multipurpose For In Vitro Coagulation Studies   More FDA Info for this Device
510(K) Number	K172333
Device Name	System, Multipurpose For In Vitro Coagulation Studies
Applicant	Siemens Healthcare Diagnostics Products GmbH Emil-von-Behring Strasse 76 Marburg 35041 DE Other 510(k) Applications for this Company
Contact	Donna Noeh Other 510(k) Applications for this Contact
Regulation Number	864.5425   More FDA Info for this Regulation Number
Classification Product Code	JPA Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/02/2017
Decision Date	10/31/2017
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HE - Hematology
Review Advisory Committee	HE - Hematology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review